3360-69-8Relevant articles and documents
Synthesis of α-aminophosphonates using solvate ionic liquids
Eyckens, Daniel J.,Henderson, Luke C.
, p. 27900 - 27904 (2017/07/07)
A range of α-aminophosphonates were accessed in high yields and very rapidly, using solvate ionic liquids as the reaction media. Reactions typically required less than 10 minutes to go to completion and precipitation of these products into water excludes the use of traditional work up procedures, giving the products in very high crude purity. Excellent functional group tolerance for both the aldehyde and amine reaction partners was observed, and a range of bis-aminophosphonates derived from aromatic diamines were also accessed in high yield and purity.
Zinc Di(l-prolinate)-Mediated Synthesis of α-Aminophosphonates under Mild Conditions
De Oliveira, Aline R.,Katla, Ramesh,Rocha, Mariana P. D.,Albuquerque, Tábata B.,Da Silva, Caren D. G.,Kupfer, Vicente L.,Rinaldi, Andrelson W.,Domingues, Nelson Luís Campos
, p. 4489 - 4494 (2016/12/16)
An efficient method has been developed for the preparation of α-aminophosphonates by using zinc di(l-prolinate) as a catalyst under mild reaction conditions. The method has the advantages of high yields, short reaction times, and easy workup conditions.
A novel and efficient synthesis of α-aminophosphonates by use of triphenyl phosphite in acetic acid media
Rostamizadeh, Mohsen,Maghsoodlou, Malek Taher,Hazeri, Nourallah,Habibi-Khorassani, Sayyed Mostafa,Keishams, Leila
experimental part, p. 334 - 337 (2011/04/24)
Chemical Equation Presented For the first time, α-aminophosphonates were obtained by a simple and efficient one-pot method from the reaction between aldehyde, aniline, and triphenyl phosphite in the presence of acetic acid as a catalyst and solvent at roo
